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143260-83-7

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143260-83-7 Usage

Also known as

3-(4-(2-hydroxyethyl)phenyl)propan-1-ol

Appearance

Colorless, viscous liquid

Industries

Pharmaceuticals, perfumes, flavors

Classification

Alcohol

Groups attached

Phenyl group, hydroxyethyl group

Applications

Fragrance ingredient, synthetic intermediate

Versatility

Used in cosmetics, personal care products, other chemicals, pharmaceuticals

Check Digit Verification of cas no

The CAS Registry Mumber 143260-83-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,3,2,6 and 0 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 143260-83:
(8*1)+(7*4)+(6*3)+(5*2)+(4*6)+(3*0)+(2*8)+(1*3)=107
107 % 10 = 7
So 143260-83-7 is a valid CAS Registry Number.

143260-83-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-[4-(2-hydroxyethyl)phenyl]propan-1-ol

1.2 Other means of identification

Product number -
Other names Benzenepropanol,4-(2-hydroxyethyl)

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:143260-83-7 SDS

143260-83-7Relevant articles and documents

Paracyclophanes: Extending the bridges. Synthesis

Pechlivanidis, Zissis,Hopf, Henning,Ernst, Ludger

experimental part, p. 223 - 237 (2009/06/21)

Preparatively satisfactory routes to [3.2]paracyclophane (10), [4.2]paracyclophane (14), [4.3]paracyclophane (19) as well as several derivatives of these compounds - among others the bromides 25, the ester 31, the diesters 40-43 - are described using well-established methods of cyclophane chemistry (ring-closure reactions leading to thiacyclophanes, ring contraction by sulfone pyrolysis). The parent systems and their derivatives are now available in gram quantities allowing a study of their chemical properties. Wiley-VCH Verlag GmbH & Co. KGaA, 2009.

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